| scholarly article | Q13442814 |
| P50 | author | Hakon Hakonarson | Q30003940 |
| P2093 | author name string | Yu Zhang | |
| Soumitra Ghosh | |||
| P2860 | cites work | Ultrafast and memory-efficient alignment of short DNA sequences to the human genome | Q21183894 |
| Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia | Q24531526 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| A map of human genome variation from population-scale sequencing | Q24617794 | ||
| Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes | Q24632382 | ||
| Fast and accurate short read alignment with Burrows-Wheeler transform | Q24653853 | ||
| The Sequence Alignment/Map format and SAMtools | Q27860966 | ||
| Pooled association tests for rare variants in exon-resequencing studies | Q28743126 | ||
| Fast and accurate long-read alignment with Burrows-Wheeler transform | Q29547193 | ||
| Next-generation DNA sequencing | Q29547447 | ||
| Common and rare variants in multifactorial susceptibility to common diseases | Q29616282 | ||
| Fank1 interacts with Jab1 and regulates cell apoptosis via the AP-1 pathway | Q33112702 | ||
| Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
| A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 | ||
| A data-adaptive sum test for disease association with multiple common or rare variants | Q33562753 | ||
| BASP1 promotes apoptosis in diabetic nephropathy. | Q33748559 | ||
| Testing for an unusual distribution of rare variants | Q33847792 | ||
| Rare-variant association testing for sequencing data with the sequence kernel association test | Q33954046 | ||
| Common vs. rare allele hypotheses for complex diseases | Q34038820 | ||
| Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes | Q34300842 | ||
| Killer cell Ig-like receptor (KIR) 3DL1 down-regulation enhances inhibition of type 1 diabetes by autoantigen-specific regulatory T cells | Q34549926 | ||
| Role of defective apoptosis in type 1 diabetes and other autoimmune diseases | Q35149114 | ||
| A general framework for detecting disease associations with rare variants in sequencing studies | Q35204927 | ||
| Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia | Q35956878 | ||
| Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies | Q36152947 | ||
| So many correlated tests, so little time! Rapid adjustment of P values for multiple correlated tests | Q36512128 | ||
| USP18 is a key regulator of the interferon-driven gene network modulating pancreatic beta cell inflammation and apoptosis | Q36525107 | ||
| Sequence kernel association tests for the combined effect of rare and common variants | Q36909285 | ||
| Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A | Q37245361 | ||
| Comparison of statistical tests for disease association with rare variants | Q38769458 | ||
| An evaluation of statistical approaches to rare variant analysis in genetic association studies | Q39941009 | ||
| A role for DHX32 in regulating T-cell apoptosis | Q40160373 | ||
| Asymptotic tests of association with multiple SNPs in linkage disequilibrium | Q41854759 | ||
| A novel bayesian graphical model for genome-wide multi-SNP association mapping | Q42137765 | ||
| Type-2 diabetes mellitus in schizophrenia: increased prevalence and major risk factor of excess mortality in a naturalistic 7-year follow-up | Q43689583 | ||
| Nuclear receptor coactivator PNRC2 regulates energy expenditure and adiposity | Q47571223 | ||
| Incidence of schizophrenia in a nationwide cohort of patients with type 1 diabetes mellitus. | Q51900842 | ||
| A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST). | Q51928874 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 12 | |
| P304 | page(s) | 867-878 | |
| P577 | publication date | 2014-09-11 | |
| P1433 | published in | Genetics | Q3100575 |
| P1476 | title | Dynamic Bayesian testing of sets of variants in complex diseases | |
| P478 | volume | 198 |
| Q47370553 | Bayesian analysis of genome-wide inflammatory bowel disease data sets reveals new risk loci | cites work | P2860 |
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